FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Lens

PMA: P910058 · Supplement: S007 · Decision Dec 14, 1995
Classifications
1
FEI Numbers
59
Registration Numbers
59

Basic Information

Device Name
Intraocular Lens
Trade Name
MODEL C11UB ULTRAVIOLET-ABSORBING SILICONE POSTERIOR CHAMBER INTRAOCULAR LENS
PMA Number
P910058
Supplement Number
S007
Device Class
FDA Class 3
Product Code
HQL
Generic Name
intraocular lens
Regulation Number
886.3600
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
December 14, 1995
Date Received
November 30, 1995
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N
Docket Number
n

Advisory Committee Statement

APPROVAL FOR MODEL C11UB ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HQL Intraocular Lens